Primary Device ID | 10840861100498 |
NIH Device Record Key | 629e0797-cc56-46f7-bb90-4087b8c00790 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MeDS Pump |
Version Model Number | 04-7103-7 |
Catalog Number | 04-7103-7 |
Company DUNS | 958291411 |
Company Name | Fresenius Medical Care Holdings, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx | |
Phone | +1(800)323-5188 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840861100491 [Primary] |
GS1 | 10840861100498 [Package] Contains: 00840861100491 Package: Case [100 Units] In Commercial Distribution |
KDI | Dialyzer, high permeability with or without sealed dialysate system |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2015-09-30 |
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